ClinVar Miner

List of variants reported as pathogenic for Alport syndrome 1, X-linked recessive by Mendelics

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Total variants: 3

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HGVS	dbSNP
NM_033380.3(COL4A5):c.2395+2T>A	rs1603293639
NM_033380.3(COL4A5):c.321+2T>G	rs1603279005
NM_033380.3(COL4A5):c.4822-1G>T	rs1603328372

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